Evidence map›Paper›PMID 38090017›Full record

ArticleJournal of osteoporosis2023

Skeletal Manifestations, Bone Pain, and BMD Changes in Albanian Type 1 Gaucher Patients Treated with Taliglucerase Alfa.

Virtut Velmishi, Erjon Troja, Marjeta Tanka, Donjeta Bali, Ermira Dervishi, Afërdita Tako, Laurant Kollcaku, Paskal Cullufi

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of osteoporosis, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Virtut VelmishiUniversity of Medicine, Pediatric Department, Gaucher Unit, "Mother Teresa Hospital", Tirana, Albania.ORCID https://orcid.org/0000-0003-1648-7258
Erjon TrojaUniversity of Medicine, Faculty of Medicine, Department of Pharmacy, Tirana, Albania.ORCID https://orcid.org/0000-0002-5632-1634
Marjeta TankaUniversity of Medicine, Pediatric Department, "Mother Teresa Hospital", Tirana, Albania.ORCID https://orcid.org/0000-0002-4874-1778
Donjeta BaliUniversity of Medicine, Pediatric Department, "Mother Teresa Hospital", Tirana, Albania.ORCID https://orcid.org/0000-0002-3528-9559
Ermira DervishiUniversity of Medicine, Pediatric Department, Gaucher Unit, "Mother Teresa Hospital", Tirana, Albania.ORCID https://orcid.org/0000-0003-3073-0277
Afërdita TakoUniversity of Medicine, Pediatric Department, "Mother Teresa Hospital", Tirana, Albania.ORCID https://orcid.org/0000-0001-9019-6390
Laurant KollcakuUniversity of Medicine, Pediatric Department, "Mother Teresa Hospital", Tirana, Albania.ORCID https://orcid.org/0000-0003-1264-7373
Paskal CullufiUniversity of Medicine, Pediatric Department, Gaucher Unit, "Mother Teresa Hospital", Tirana, Albania.ORCID https://orcid.org/0000-0001-5678-9926
Mother Teresa Hospital · ALUniversity of Medicine Tirana · AL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gaucher disease is a rare, genetic lysosomal disorder leading to lipid accumulation and dysfunctions in multiple organs. Bone involvement is one of the most prevalent aspects of Gaucher disease. Pain, disability, and reduced quality of life remain the most frequent characteristics of bone involvement in Gaucher patients.

Identifiers

PMID38090017
PMCPMC10713248
OpenAlexW4389312154

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.